Slco1b2 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slco1b2
solute carrier organic anion transporter family, member 1b2
MGI:1351899

17 phenotypes from 2 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Slco1b2^em1(IMPC)Mbp/Slco1b2^em1(IMPC)Mbp C57BL/6NCrl-Slco1b2^em1(IMPC)Mbp/MbpMmucd	abnormal eye morphology	J:211773
	abnormal skin morphology	J:211773
	increased circulating bilirubin level	J:211773
	increased red blood cell distribution width	J:211773
Slco1b2^tm1Cdk/Slco1b2^tm1Cdk B6.129S1-Slco1b2^tm1Cdk	abnormal circulating mineral level	J:133919
	abnormal circulating protein level	J:133919
	abnormal circulating serum albumin level	J:133919
	abnormal liver physiology	J:133919
	decreased circulating amylase level	J:133919
	decreased physiological sensitivity to xenobiotic	J:133919
	decreased susceptibility to xenobiotic induced morbidity/mortality	J:133919
	increased circulating alanine transaminase level	J:133919
	increased circulating bilirubin level	J:133919
	increased circulating chloride level	J:133919
	increased circulating cholesterol level	J:133919
	increased circulating sodium level	J:133919
	increased circulating total protein level	J:133919
Slco1b2^tm1Cdk/Slco1b2^tm1Cdk involves: 129S1/Sv * C57BL/6	abnormal liver physiology	J:133919
	abnormal xenobiotic pharmacokinetics	J:133919
	decreased physiological sensitivity to xenobiotic	J:133919

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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